K-number	K970438
Device name	INTERLINK MICRO-INFUSION MANIFOLD EXTENSION SETS
Applicant	Baxter Healthcare Corp
Product code	FPA
Device class	Class II
Decision date	Apr 2, 1997
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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INTERLINK MICRO-INFUSION MANIFOLD EXTENSION SETS

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